Ö. Sanal

I. Tezcan, M. Yılmaz, Ö. Sanal, 2014, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients

I. Tezcan, Ö. Sanal, A. Metin, 2012, European Journal of Pediatrics.

Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing

O. Sanal, I. Tezcan, I. Bilic, 2017, Scandinavian journal of immunology.

Immune deficiencies , infection , and systemic immune disorders Mutations in STAT 3 and diagnostic guidelines for hyper-IgE syndrome

A. Schäffer, A. Plebani, C. Pignata, 2010 .

Successful hematopoietic stem cell transplantation after myeloablative conditioning in three patients with dedicator of cytokinesis 8 deficiency (DOCK8) related Hyper IgE syndrome

I. Tezcan, D. Çetinkaya, A. Yüce, 2018, Bone Marrow Transplantation.

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

J. Orange, A. Schulz, R. Geha, 2015, Journal of Clinical Immunology.

Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS.

I. Tezcan, Ö. Sanal, Çağman Tan, 2015, The Turkish journal of pediatrics.

Low T Cell Numbers Resembling T−B+ SCID in a Patient with Wiskott–Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations

I. Tezcan, T. Ariga, D. Çetinkaya, 2016, Journal of Clinical Immunology.

PARVOVIRUS B19-INDUCED PERSISTENT PURE RED CELL APLASIA IN A CHILD WITH T-CELL IMMUNODEFICIENCY

Ö. Sanal, F. Gumruk, A. Gurgey, 2009, Pediatric hematology and oncology.

Molecular analysis of an MHC class II deficiency patient reveals a novel mutation in the RFX5 gene

P. J. van den Elsen, A. Peijnenburg, Ö. Sanal, 1999, Immunogenetics.

IgG subclasses in children with recurrent respiratory tract infections in an allergy practice

F. Ersoy, Ö. Sanal, B. Sekerel, 1996, Acta paediatrica Japonica : Overseas edition.

Selective IgA deficiency with unusual features: Development of common variable immunodeficiency, Sjögren's syndrome, autoimmune hemolytic anemia and immune thrombocytopenic purpura

I. Tezcan, F. Ersoy, Ö. Sanal, 1995, Acta paediatrica Japonica : Overseas edition.

Hyperimmunoglobulinemia D and periodic fever syndrome; treatment with etanercept and follow-up

H. Waterham, R. Topaloğlu, A. Yüce, 2008, Clinical Rheumatology.

Hematopoietic Stem Cell Transplantation as Treatment for Patients with DOCK8 Deficiency.

J. Ziegler, A. Schulz, R. Geha, 2019, The journal of allergy and clinical immunology. In practice.

Two SCID cases with Cernunnos‐XLF deficiency successfully treated by hematopoietic stem cell transplantation

M. van der Burg, P. Revy, I. Tezcan, 2012, Pediatric transplantation.

Hodgkin's disease and ataxia telangiectasia with pulmonary cavities

B. Yalçın, M. Çağlar, Ö. Sanal, 2002, Pediatric Pulmonology.

MALIGNANT SOLID TUMORS ASSOCIATED WITH CONGENITAL IMMUNODEFICIENCY DISORDERS

F. Ersoy, A. Varan, B. Yalçın, 2004, Pediatric hematology and oncology.

Atypical combined immunodeficiency due to Artemis defect: a case presenting as hyperimmunoglobulin M syndrome and with LGLL.

I. Tezcan, J. de Villartay, D. Ayvaz, 2013, Molecular immunology.

A single‐center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class‐ Switch Recombination defects

I. Tezcan, Ö. Sanal, D. Çağdaş, 2022, Scandinavian journal of immunology.

Defective pneumococcal antibody response in patients with recurrent respiratory tract infections.

I. Tezcan, Ö. Sanal, B. Erman, 2017, The Turkish journal of pediatrics.

B lymphocyte subsets and outcomes in patients with an initial diagnosis of transient hypogammaglobulinemia of infancy

I. Tezcan, Ö. Sanal, F. K. Eroğlu, 2018, Scandinavian journal of immunology.

An infant with severe leucocyte adhesion deficiency

Ö. Sanal, S. Güneşer, P. Aksungur, 1996, Acta paediatrica.

A Novel Mutation in the Complement Component 3 Gene in a Patient with Selective IgA Deficiency

K. Boztug, H. Artaç, Ö. Sanal, 2012, Journal of Clinical Immunology.

Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome.

A. Schäffer, E. Gertz, A. Plebani, 2010, The Journal of allergy and clinical immunology.

Hodgkin's disease and ataxia telangiectasia with pulmonary cavities

B. Yalçın, Ö. Sanal, M. T. Kutluk, 2002, Pediatric Pulmonology.

CLINICAL FEATURES OF CANDIDIASIS IN PATIENTS WITH INTERLEUKIN-12 RECEPTOR B1 DEFICIENCY

J. Casanova, C. Picard, L. Abel, 2012 .

Genetic analysis of patients with leukocyte adhesion deficiency: genomic sequencing reveals otherwise undetectable mutations.

O. Sanal, I. Tezcan, C. Meischl, 2002, Experimental hematology.

Interleukin‐12/‐23 receptor beta 1 deficiency in an infant with draining BCG lymphadenitis

S. Asilsoy, D. Can, Ö. Sanal, 2009, Pediatrics international : official journal of the Japan Pediatric Society.